Human IgG1&Igκ Isotype Recombinant Monoclonal Antibody

Code CSB-RA011156MA1HU
Size US$210
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  • Untransfected MC38 cells and transfected Human TSPAN8 MC38 stable cells were stained with Human IgG1&Igκ Isotype Control (CSB-RA011156MA1HU) and anti-TSPAN8 antibody (CSB-RA025166MA1HU) (2µg/1*106cells), washed and then followed by FITC-conjugated anti-Human IgG Fc antibody and analyzed with flow cytometry.
  • HT29 cells were stained with Human IgG1&Igκ Isotype Control (CSB-RA011156MA1HU)(green line) and anti-TSPAN8 antibody (CSB-RA882142MA1HU) (2µg/1*106cells) (red line), washed and then followed by FITC-conjugated anti-Human IgG Fc antibody and analyzed with flow cytometry.
  • The purity of Human IgG1&Igκ Isotype was greater than 95% as determined by SEC-HPLC
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Product Details

Uniprot No.
Target Names
IgG1
Alternative Names
Human IgG1
Species Reactivity
Human
Immunogen
Recombinant Human IgG1 protein
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Monoclonal
Isotype
hIgG1
Clone No.
4D2
Purification Method
Affinity-chromatography
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Form
Liquid
Tested Applications
FC
Recommended Dilution
Application Recommended Dilution
FC 1:50-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Description

Isotype controls serve as essential negative controls in flow cytometry and immunostaining experiments, enabling researchers to distinguish true antigen-specific signals from background fluorescence caused by non-specific antibody binding. This Human IgG1 and Igκ Isotype Recombinant Monoclonal Antibody provides the critical baseline reference needed to validate experimental results and ensure accurate interpretation of data when using human IgG1 primary antibodies.

Developed using recombinant technology with clone 4D2, this isotype control offers the consistency and reproducibility that rigorous experimental design demands. Unlike traditional hybridoma-derived antibodies, recombinant production ensures sequence-defined specificity and eliminates the lot-to-lot variability that can compromise longitudinal studies or multi-site collaborations. The antibody undergoes affinity chromatography purification, achieving greater than 95% purity as confirmed by SEC-HPLC analysis.

This isotype control has been validated for flow cytometry applications at recommended dilutions of 1:50 to 1:200. Experimental testing demonstrates its utility as a proper negative control alongside TSPAN8-targeting antibodies, with validation performed using both untransfected and transfected MC38 stable cells, as well as HT29 cells. In these experiments, the isotype control established clear baseline fluorescence levels when detected with FITC-conjugated anti-Human IgG Fc secondary antibody, allowing for confident discrimination of specific TSPAN8 staining.

Supplied in a liquid format containing 50% glycerol and PBS at pH 7.4 with Proclin 300 preservative, this antibody maintains stability when stored at -20°C or -80°C. Researchers working in immunology and stem cell biology will find this isotype control indispensable for generating publication-quality flow cytometry data with properly controlled experimental conditions.

Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function
Constant region of immunoglobulin heavy chains. Immunoglobulins, also known as antibodies, are membrane-bound or secreted glycoproteins produced by B lymphocytes. In the recognition phase of humoral immunity, the membrane-bound immunoglobulins serve as receptors which, upon binding of a specific antigen, trigger the clonal expansion and differentiation of B lymphocytes into immunoglobulins-secreting plasma cells. Secreted immunoglobulins mediate the effector phase of humoral immunity, which results in the elimination of bound antigens. The antigen binding site is formed by the variable domain of one heavy chain, together with that of its associated light chain. Thus, each immunoglobulin has two antigen binding sites with remarkable affinity for a particular antigen. The variable domains are assembled by a process called V-(D)-J rearrangement and can then be subjected to somatic hypermutations which, after exposure to antigen and selection, allow affinity maturation for a particular antigen.
Involvement in disease
Multiple myeloma (MM)
Subcellular Location
Secreted. Cell membrane.
Database Links

HGNC: 5525

OMIM: 147100

UniGene: Hs.510635

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Address
No. 269, Shendun 5th Road, Donghu Hi-Tech Development Area, Hubei Province, 430206, P.R.China
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